Diethyl Ether → HCID 14976040, compound
Reaction equation
[Br:1][CH2:2][CH2:3][CH2:4][OH:5].[CH3:6][S:7](Cl)(=[O:9])=[O:8].CCOCC>C(N(CC)CC)C>[CH3:6][S:7]([O:5][CH2:4][CH2:3][CH2:2][Br:1])(=[O:9])=[O:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture containing 13.9 ml. of 3-bromo-1-propanol, 7.6 ml. of methane sulfonyl chloride and 100 ml. ether was formed. The mixture was mixed together and 14 ml. of triethylamine was added over a period of 45 minutes at 5°-10° C. and then stirred at 5°-10° C. for 1 hour. The mixture was allowed to come to room temperature and was stirred for an additional 15 minutes. To the mixture was added 100 ml. of water and the ether solution dried over magnesium sulfate and evaporated to yield 14.5 g. of a colorless oil. nD30 1.4749.
Workup
- additionA mixture containing 13.9 ml
- additionThe mixture was mixed together
- customto come to room temperature
- stirringwas stirred for an additional 15 minutes
- additionTo the mixture was added 100 ml
- dry with materialof water and the ether solution dried over magnesium sulfate
- customevaporated
- customto yield 14.5 g
Sources & evidence
- ORD record
- ord-854f6c8cd12b4fc888a266476108c158
- Source dataset
- uspto-grants-1978_07
- Patent number
- US04098599
Reaction notes
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